BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    MODIFIED MEMORY RETRACTOR ARM

    FDA 510(k)
    FDA Class 2 ·Neurology

    GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CORE BIOPSY NEEDLE, CATALOG CODE #54006

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·January 3, 2013

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 10, 2010

    AIMING ARM FOR TI CANNULATED TIBIAL NAILS-EX

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code FZX·July 7, 2015